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Metabolic Brain Disease|August 6, 2021
Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous MalformationsSilvia Lanfranconi, Lorenzo Piergallini, Dario Ronchi, et al.Immunity|May 28, 2013
A 175 million year history of T cell regulatory molecules reveals widespread selection, with adaptive evolution of disease allelesDiego Forni, Rachele Cagliani, Uberto Pozzoli, et al.Atherosclerosis|November 28, 2017
Subclinical cerebrovascular disease in NAFLD without overt risk factors for atherosclerosisLorena Airaghi, Mario Rango, Diletta Maira, et al.Journal of the Neurological Sciences|September 20, 2005
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsyMonica Sciacco, Alessandro Prelle, Gigliola Fagiolari, et al.Annals of Neurology|May 16, 2007
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis miceFederica Locatelli, Stefania Corti, Dimitra Papadimitriou, et al.Journal of the Neurological Sciences|December 27, 2011
Optic atrophy plus phenotype due to mutations in the OPA1 gene: two more Italian familiesMichela Ranieri, Roberto Del Bo, Andreina Bordoni, et al.BMC Neurology|September 26, 2015
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy casesFrancesca Magri, Irene Colombo, Roberto Del Bo, et al.Journal of Alzheimer'S Disease : JAD|May 11, 2012
Early onset behavioral variant frontotemporal dementia due to the C9ORF72 hexanucleotide repeat expansion: psychiatric clinical presentationsAndrea Arighi, Giorgio G Fumagalli, Francesca Jacini, et al.Brain : a Journal of Neurology|December 25, 2009
Embryonic stem cell-derived neural stem cells improve spinal muscular atrophy phenotype in miceStefania Corti, Monica Nizzardo, Martina Nardini, et al.Science (New York, N.Y.)|July 12, 2003
Cell therapy of alpha-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblastsMaurilio Sampaolesi, Yvan Torrente, Anna Innocenzi, et al.Pageof 34